Does CANDESARTAN Cause Intentional product misuse? 319 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 319 reports of Intentional product misuse have been filed in association with CANDESARTAN. This represents 3.5% of all adverse event reports for CANDESARTAN.
319
Reports of Intentional product misuse with CANDESARTAN
3.5%
of all CANDESARTAN reports
31
Deaths
123
Hospitalizations
How Dangerous Is Intentional product misuse From CANDESARTAN?
Of the 319 reports, 31 (9.7%) resulted in death, 123 (38.6%) required hospitalization, and 106 (33.2%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CANDESARTAN. However, 319 reports have been filed with the FAERS database.
What Other Side Effects Does CANDESARTAN Cause?
Off label use (1,911)
Fatigue (1,468)
Dyspnoea (1,456)
Pain (1,455)
Drug ineffective (1,428)
Headache (1,371)
Nausea (1,282)
Dizziness (1,237)
Vomiting (1,202)
Diarrhoea (1,145)
What Other Drugs Cause Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which CANDESARTAN Alternatives Have Lower Intentional product misuse Risk?
CANDESARTAN vs CANDESARTAN CILEXETIL
CANDESARTAN vs CANDESARTAN CILEXETIL\HYDROCHLOROTHIAZIDE
CANDESARTAN vs CANGRELOR
CANDESARTAN vs CANIS LUPUS FAMILIARIS SKIN
CANDESARTAN vs CANNABIDIOL